Whole-Exome Sequencing Identifies Mutations of KIF22 in Spondyloepimetaphyseal Dysplasia with Joint Laxity, Leptodactylic Type

Byung-Joo Min(Seoul National University), Tae‐Joon Cho(Seoul National University Children's Hospital), Jong‐Il Kim(Seoul National University), Gen Nishimura(Musashino University), Jeong‐Sun Seo(Seoul National University), Daehee Kang(Seoul National University), Taehoon Kang(Seoul National University Hospital), Taesu Chung(Korea Advanced Institute of Science and Technology), Dongsup Kim(Korea Advanced Institute of Science and Technology), Ji‐Yeob Choi(Seoul National University), Woong‐Yang Park(Samsung Medical Center), Chin Youb Chung(Seoul National University), Ok-Hwa Kim(Korea University Medical Center), Hyun Woo Kim(Severance Hospital), Jiwoong Kim(The University of Texas Southwestern Medical Center), Do-Hwan Kim(Seoul National University), Seungbok Lee(Seoul National University), Hyeran Lee(Mokwon University), Myung-Eui Seo(Seoul National University), Hae Ryong Song(Korea University Medical Center), San‐Duk Yang(Ewha Womans University), Namshin Kim(Korea Research Institute of Bioscience and Biotechnology)
The American Journal of Human Genetics
December 1, 2011
Cited by 62


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